Viral hepatitis B and C infections increase the risks of intrahepatic and extrahepatic cholangiocarcinoma: Evidence from a systematic review and meta-analysis.
Adult
Aged
Antigens, Tumor-Associated, Carbohydrate
/ blood
Bile Duct Neoplasms
/ epidemiology
Bile Ducts, Extrahepatic
/ virology
Bile Ducts, Intrahepatic
/ virology
Cholangiocarcinoma
/ epidemiology
Female
Hepacivirus
Hepatitis B
/ complications
Hepatitis B virus
Hepatitis C
/ complications
Humans
Lymph Nodes
/ virology
Male
Middle Aged
Risk Factors
alpha-Fetoproteins
/ metabolism
Journal
The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology
ISSN: 2148-5607
Titre abrégé: Turk J Gastroenterol
Pays: Turkey
ID NLM: 9515841
Informations de publication
Date de publication:
03 2020
03 2020
Historique:
entrez:
29
4
2020
pubmed:
29
4
2020
medline:
8
10
2021
Statut:
ppublish
Résumé
Previous study has shown a positive relationship between the hepatitis B virus (HBV) or hepatitis C virus (HCV) infection and cholangiocarcinoma (CCA); however, their correlation with different anatomical sites of CCA (i.e. ICC and ECC) has not been revealed. This study aims to evaluate the association of HBV or HCV infection with CCA, including the intrahepatic cholangiocarcinoma (ICC) and extrahepatic cholangiocarcinoma (ECC), and to determine the roles of α-1 fetoprotein (AFP), CA19-9, and lymph node involvement in CCA with HBV infection. Relevant studies published between 2004 and 2016 were systematically searched and retrieved from PubMed, SpringerLink, and Science Direct using key terms such as "cholangiocarcinoma", "bile duct cancer", "extrahepatic cholangiocarcinoma", and "intrahepatic cholangiocarcinoma". The demographic, clinical, and laboratory data were extracted from the included studies, and the meta-analysis was performed using RevMan and STATA 11.0 software. A total of 13 studies with CCA matched the inclusion criteria in this meta-analysis, including 7,113 CCA patients and 24,763 controls. This meta-analysis showed that the HBV or HCV infections can significantly increase the risk of CCA, including ICC and ECC. In addition, the higher levels of AFP, lower levels of CA19-9, and lymph node involvement were detected in the CCA patients with HBV infection as compared to those without. The HBV and HCV infections significantly increased the risk of CCA, as well as ICC and ECC. The involvement of AFP, CA19-9, and lymph nodes may play an important role in the diagnosis of CCA.
Sections du résumé
BACKGROUND/AIMS
Previous study has shown a positive relationship between the hepatitis B virus (HBV) or hepatitis C virus (HCV) infection and cholangiocarcinoma (CCA); however, their correlation with different anatomical sites of CCA (i.e. ICC and ECC) has not been revealed. This study aims to evaluate the association of HBV or HCV infection with CCA, including the intrahepatic cholangiocarcinoma (ICC) and extrahepatic cholangiocarcinoma (ECC), and to determine the roles of α-1 fetoprotein (AFP), CA19-9, and lymph node involvement in CCA with HBV infection.
MATERIALS AND METHODS
Relevant studies published between 2004 and 2016 were systematically searched and retrieved from PubMed, SpringerLink, and Science Direct using key terms such as "cholangiocarcinoma", "bile duct cancer", "extrahepatic cholangiocarcinoma", and "intrahepatic cholangiocarcinoma". The demographic, clinical, and laboratory data were extracted from the included studies, and the meta-analysis was performed using RevMan and STATA 11.0 software.
RESULTS
A total of 13 studies with CCA matched the inclusion criteria in this meta-analysis, including 7,113 CCA patients and 24,763 controls. This meta-analysis showed that the HBV or HCV infections can significantly increase the risk of CCA, including ICC and ECC. In addition, the higher levels of AFP, lower levels of CA19-9, and lymph node involvement were detected in the CCA patients with HBV infection as compared to those without.
CONCLUSION
The HBV and HCV infections significantly increased the risk of CCA, as well as ICC and ECC. The involvement of AFP, CA19-9, and lymph nodes may play an important role in the diagnosis of CCA.
Identifiants
pubmed: 32343237
doi: 10.5152/tjg.2020.19056
pmc: PMC7197930
doi:
Substances chimiques
AFP protein, human
0
Antigens, Tumor-Associated, Carbohydrate
0
alpha-Fetoproteins
0
carbohydrate antigen 199, human
0
Types de publication
Journal Article
Meta-Analysis
Research Support, Non-U.S. Gov't
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
246-256Références
Asian Pac J Cancer Prev. 2010;11(4):985-8
pubmed: 21133611
Ann Oncol. 2013 Jun;24(6):1667-74
pubmed: 23378539
World J Gastroenterol. 2015 Jan 14;21(2):502-10
pubmed: 25593465
Ann Surg Oncol. 2011 May;18(5):1258-66
pubmed: 21207172
Stem Cell Rev. 2005;1(3):253-60
pubmed: 17142862
PLoS One. 2013 Jul 22;8(7):e69981
pubmed: 23894567
Hepatobiliary Surg Nutr. 2013 Oct;2(5):272-80
pubmed: 24570958
Ann Surg. 2008 Jul;248(1):84-96
pubmed: 18580211
Ann Surg. 2011 Nov;254(5):824-29; discussion 830
pubmed: 22042474
World J Gastroenterol. 2016 Mar 14;22(10):3038-51
pubmed: 26973400
Asian Pac J Cancer Prev. 2012;13(5):1963-9
pubmed: 22901155
BMJ. 2011 Oct 18;343:d5928
pubmed: 22008217
World J Gastroenterol. 2014 Sep 21;20(35):12615-20
pubmed: 25253966
Clin Res Hepatol Gastroenterol. 2016 Dec;40(6):682-687
pubmed: 27282820
Scand J Gastroenterol. 2011 Sep;46(9):1092-8
pubmed: 21692710
J Gastroenterol Hepatol. 2012 Oct;27(10):1561-8
pubmed: 22694354
Intern Med. 2014;53(7):651-4
pubmed: 24694471
Biomed Res Int. 2016;2016:3417976
pubmed: 27999794
Am J Gastroenterol. 2000 Jan;95(1):204-7
pubmed: 10638584
Eur J Epidemiol. 2010 Sep;25(9):603-5
pubmed: 20652370
Hepatology. 2001 Jun;33(6):1353-7
pubmed: 11391522
Cancer Cell Int. 2013 Oct 18;13(1):99
pubmed: 24139471
Eur J Cancer. 2010 Apr;46(6):1056-61
pubmed: 20202823
Int J Cancer. 2013 Oct 15;133(8):1867-75
pubmed: 23564396
World J Gastroenterol. 2011 Jan 14;17(2):249-53
pubmed: 21246000
J Hepatol. 2017 Jan;66(1):48-54
pubmed: 27592304
JAMA. 2000 Apr 19;283(15):2008-12
pubmed: 10789670
Asia Pac J Clin Oncol. 2012 Mar;8(1):83-7
pubmed: 22369448
ANZ J Surg. 2018 Mar;88(3):212-217
pubmed: 27598539